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. 2024 Jun;11(3):1540-1552.
doi: 10.1002/ehf2.14611. Epub 2024 Jan 15.

Impact of rapid sequential combination therapy on distinct haemodynamic measures in newly diagnosed pulmonary arterial hypertension

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Impact of rapid sequential combination therapy on distinct haemodynamic measures in newly diagnosed pulmonary arterial hypertension

Tilmann Kramer et al. ESC Heart Fail. 2024 Jun.

Abstract

Aims: In pulmonary arterial hypertension (PAH), upfront combination therapy with ERA and PDE5i is associated with a reduction in morbidity and mortality events and improves standard haemodynamics, but data remain limited. Aims of this study were (i) to capture detailed haemodynamic effects of rapid sequential dual combination therapy in patients with newly diagnosed PAH; (ii) to monitor the impact of treatment initiation on clinical variables and patients' risk status, and (iii) to compare the treatment effect in patients with 'classical PAH' and 'PAH with co-morbidities'.

Methods: Fifty patients (median age 57 [42-71] years, 66% female) with newly diagnosed PAH (76% idiopathic) were treated with a PD5i/sGC-S or ERA, followed by addition of the respective other drug class within 4 weeks. All patients underwent repeat right heart catheterization (RHC) during early follow-up.

Results: At early repeat RHC (7 ± 2 months), there were substantial reductions in mean pulmonary artery pressure (mPAP: 52.2 ± 13.5 to 39.0 ± 10.6 mmHg; -25.3%), and pulmonary vascular resistance (PVR: 12.1 ± 5.7 to 5.8 ± 3.1 WU; -52.1%), and an increase in cardiac index (2.1 ± 0.4 to 2.7 ± 0.7 mL/min/m2; +32.2%) (all P < 0.05). Haemodynamic improvements correlated with improved clinical parameters including 6-min walking distance (336 ± 315 to 389 ± 120 m), NTproBNP levels (1.712 ± 2.024 to 506 ± 550 ng/L, both P < 0.05) and WHO-FC at 12 months, resulting in improved risk status, and were found in patients with few (n = 37) or multiple cardiovascular co-morbidities (BMI > 30 kg/m2, hypertension, diabetes, coronary artery disease [≥3]; n = 13), albeit baseline PVR in PAH patients with multiple co-morbidities was lower (9.3 ± 4.4 vs. 13.1 ± 5.9 WU) and PVR reduction less pronounced compared with those with few co-morbidities (-42.7% vs. -54.7%). However, comprehensive haemodynamic assessment considering further variables of prognostic relevance such as stroke volume index and pulmonary artery compliance showed similar improvements among the two groups (SVI: +50.0% vs. +49.2%; PAC: 91.7% vs. 100.0%). Finally, the 4-strata risk assessment approach was better able to capture treatment response as compared with other approaches, particularly in patients with co-morbidities.

Conclusions: Rapid sequential combination therapy with PDE5i/sGC-S and ERA substantially ameliorates cardiopulmonary haemodynamics at early follow-up in patients without, and to a lesser extent, with cardiovascular co-morbidities. This occurs in line with improvements of clinical parameters and risk status.

Keywords: Combination therapy; Endothelin receptor antagonist; Haemodynamics; Phosphodiesterase type 5 inhibitor; Pulmonary arterial hypertension (PAH).

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Conflict of interest statement

Tilmann Kramer: Remunerations for lectures from Actelion. Felix Gerhardt: Remunerations for lectures from Actelion, Bayer, GSK, and United Therapeutics; grants to institution from Actelion, Bayer, Novartis, and United Therapeutics. Daniel Dumitrescu: Remunerations for lectures and/or consultancy from Actelion, Bayer, GSK, MSD, Novartis, Servier, and Vifor. Christopher Hohmann: Personal fees from MSD and Pfizer, lecture fees from Actelion, travel grants from Actelion, Bayer, Orion Pharma, and MSD. Stephan Rosenkranz: Remunerations for lectures and/or consultancy from Abbott, Acceleron, Actelion, Aerovate, Altavant, AOP, AstraZeneca, Bayer, Boehringer‐Ingelheim, BMS, Ferrer, Gossamer, MSD, Novartis, Pfizer, United Therapeutics, and Vifor; grants to institution from Actelion, AstraZeneca, Bayer, and Janssen. The rest of the authors have nothing to disclose.

Figures

Figure 1
Figure 1
Improvement of key pulmonary haemodynamics from baseline to early follow‐up as assessed by repeat right heart catheterization. Data represent mean values ± SEM. PAC, pulmonary artery compliance; PAPm, mean pulmonary artery pressure; PVR, pulmonary vascular resistance; RAP, right atrial pressure; SVI, stroke volume index.
Figure 2
Figure 2
Risk stratification according to the ESC/ERS guidelines 3‐strata approach, utilizing the SPAHR methodology of analysis. Data are shown according to patients' age. (A) Risk assessment at baseline. (B) Risk assessment at follow‐up (6 months). (C) Changes in risk assessment between baseline and follow‐up.
Figure 3
Figure 3
Risk stratification according to the ESC/ERS guidelines, utilizing the FNPH methodology of analysis which focusses on low risk criteria only. (A) Analysis based on the course of 4 criteria (including RHC) at baseline and 6 months of follow‐up. (B) Analysis based on the course of 3 criteria (non‐invasive) at baseline and 6 months of follow‐up.
Figure 4
Figure 4
Risk stratification according to the ESC/ERS guidelines 4‐strata approach at baseline, 6 and 12 months of follow‐up.

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